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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 1
2001 2
2002 2
2003 1
2004 5
2005 2
2006 6
2007 3
2008 3
2009 3
2010 5
2011 1
2012 5
2013 5
2014 3
2015 3
2016 3
2017 3
2018 2
2019 1
2021 1
2023 1
2024 0

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Page 1
ATP2B2 de novo variants as a cause of variable neurodevelopmental disorders that feature dystonia, ataxia, intellectual disability, behavioral symptoms, and seizures.
Poggio E, Barazzuol L, Salmaso A, Milani C, Deligiannopoulou A, Cazorla ÁG, Jang SS, Juliá-Palacios N, Keren B, Kopajtich R, Lynch SA, Mignot C, Moorwood C, Neuhofer C, Nigro V, Oostra A, Prokisch H, Saillour V, Schuermans N, Torella A, Verloo P, Yazbeck E, Zollino M, Jech R, Winkelmann J, Necpal J, Calì T, Brini M, Zech M. Poggio E, et al. Genet Med. 2023 Dec;25(12):100971. doi: 10.1016/j.gim.2023.100971. Epub 2023 Sep 4. Genet Med. 2023. PMID: 37675773
Two ENU-induced alleles of Atp2b2 cause deafness in mice.
Carpinelli MR, Manning MG, Kile BT, Burt RA. Carpinelli MR, et al. PLoS One. 2013 Jun 24;8(6):e67479. doi: 10.1371/journal.pone.0067479. Print 2013. PLoS One. 2013. PMID: 23826306 Free PMC article.
Phenotypes of SERCA and PMCA knockout mice.
Prasad V, Okunade GW, Miller ML, Shull GE. Prasad V, et al. Biochem Biophys Res Commun. 2004 Oct 1;322(4):1192-203. doi: 10.1016/j.bbrc.2004.07.156. Biochem Biophys Res Commun. 2004. PMID: 15336967 Review.
55 results